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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 504632Generated: October 26, 2026

Ethanol → 4-Amino-3-(benzylthio)-3-methylbutan-1-ol

https://huagongshe.com/reaction/504632

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantWaterHCID 962—
ReactantAluminium lithium hydrideHCID 21226445—
Reactant3-(Benzylthio)-3-methyl-4-nitrobutan-1-olHCID 57475976—
SolventTetrahydrofuranHCID 8028—
Product4-Amino-3-(benzylthio)-3-methylbutan-1-olHCID 5747597799%

Reaction Steps

To a mixture of lithium aluminum hydride (1.67 g) and tetrahydrofuran (30 ml) was added a solution of 3-(benzylthio)-3-methyl-4-nitrobutan-1-ol (3.00 g) in tetrahydrofuran (10 ml) over 1 hr at room temperature. The reaction mixture was stirred at room temperature for 1 hr, ethanol (10 ml) and water (6.4 ml) were added in this order, and the resulting inorganic salt was removed by filtration. The filtrate was concentrated, and the residue was dissolved in ethyl acetate, dried (MgSO4), and concentrated to give the title compound (2.62 g, yield 99%) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07777047B2
Source datasetuspto-grants-2010_08
ORD IDord-3cd60dcd841341fd812b8d2572c021be
Source noteuspto-grants-2010_08